All diseases

OMIM ID
601820
OMIM term:
HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2; HHF2
Alternative terms:
PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PHHI
HYPERINSULINEMIC HYPOGLYCEMIA, PERSISTENT
HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA
HYPERINSULINISM, NEONATAL
HYPERINSULINISM, CONGENITAL
HYPERINSULINISM, FAMILIAL
NESIDIOBLASTOSIS
(∗) Location:
11p15.1  
(†) Associated OMIM genes:
KCNJ11  
(‡) Associated MGI genes:
Gck  

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* quick link - http://q.sanger.ac.uk/x81ra023